Chemistry Atoms First2e
2nd Edition
ISBN: 9781947172647
Author: OpenStax
Publisher: OpenStax College
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Textbook Question
Chapter 21, Problem 49E
Write the two-resonance structures for the acetate ion.
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Chapter 21 Solutions
Chemistry Atoms First2e
Ch. 21 - Write the chemical formula and Lewis structure of...Ch. 21 - What is the difference between the hybridization...Ch. 21 - On a microscopic level, how does the reaction of...Ch. 21 - On a microscopic level, how does the reaction of...Ch. 21 - Explain why unbranched alkenes can form geometric...Ch. 21 - Explain why these two molecules are not isomers:Ch. 21 - Explain why these two molecules are not isomers:Ch. 21 - How does the carbon-atom hybridization change when...Ch. 21 - Write the Lewis structure and molecular formula...Ch. 21 - Write the chemical formula, condensed formula, and...
Ch. 21 - Give the complete IUPAC name for each of the...Ch. 21 - Give the complete IUPAC name for each of the...Ch. 21 - Butane is used as a fuel in disposable lighters....Ch. 21 - Write Lewis structures and name the five...Ch. 21 - Write Lewis structures for the Cis -trans isomers...Ch. 21 - Write structures for the three isomers of the...Ch. 21 - Isooctane is the common name of the isomer of...Ch. 21 - Write Lewis structures and IUPAC names for the...Ch. 21 - Write Lewis structures and IUPAC names for all...Ch. 21 - Name and write the structures of all isomers of...Ch. 21 - Write the structures for all the isomers of the...Ch. 21 - Write Lewis structures and describe the molecular...Ch. 21 - Benzene is one of the compounds used as an octane...Ch. 21 - Teflon is prepared by the polymerization of...Ch. 21 - Write two complete, balanced equations for each of...Ch. 21 - Write two complete, balanced equations for each of...Ch. 21 - What mass of 2-bromopropane could be prepared from...Ch. 21 - Acetylene is a very weak acid; however, it will...Ch. 21 - Ethylene can be produced by the pyrolysis of...Ch. 21 - Why do the compounds hexane, hexanol, and hexane...Ch. 21 - Write condensed formulas and provide IUPAC names...Ch. 21 - Give the complete IUPAC name for each of the...Ch. 21 - Give the complete IUPAC name and the common name...Ch. 21 - Write the condensed structures of both isomers...Ch. 21 - Write the condensed structures of all isomers with...Ch. 21 - Draw the condensed formulas for each of the...Ch. 21 - MTBE, Methyl tert -butyl ether, CH3OC(CH3)3, is...Ch. 21 - Write two complete balanced equations for each of...Ch. 21 - Write two complete balanced equations for each of...Ch. 21 - Order the following molecules from least to most...Ch. 21 - Predict the products of oxidizing the molecules...Ch. 21 - Predict the products of reducing the following...Ch. 21 - Explain why it is not possible to possible a...Ch. 21 - How does hybridization of the substituted carbon...Ch. 21 - Fatty acids are carboxylic acids that have long...Ch. 21 - Write a condensed structural formula, such as...Ch. 21 - Write a condensed structural formula, such as...Ch. 21 - The foul odor of rancid butter is caused by...Ch. 21 - Write the two-resonance structures for the acetate...Ch. 21 - Write two complete, balanced equations for each of...Ch. 21 - Write two complete balanced equations for each of...Ch. 21 - Yields in organic reactions are sometimes low....Ch. 21 - Alcohols A, B and C all have the composition C4H...Ch. 21 - Write the Lewis structures of both isomers with...Ch. 21 - What is the molecular structure about the nitrogen...Ch. 21 - Write the two resonance structures for the...Ch. 21 - Draw Lewis structures for pyridine and its...Ch. 21 - Write the Lewis structures of all isomers with the...Ch. 21 - Write two complete balanced equations for the...Ch. 21 - Write two complete, balanced equations for each of...Ch. 21 - Identify any carbon atoms that change...Ch. 21 - Identify any carbon atoms that change...Ch. 21 - Identify any carbon atoms that change...
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- Use the References to access important values if needed for this question. What is the IUPAC name of each of the the following? 0 CH3CHCNH₂ CH3 CH3CHCNHCH2CH3 CH3arrow_forwardYou have now performed a liquid-liquid extraction protocol in Experiment 4. In doing so, you manipulated and exploited the acid-base chemistry of one or more of the compounds in your mixture to facilitate their separation into different phases. The key to understanding how liquid- liquid extractions work is by knowing which layer a compound is in, and in what protonation state. The following liquid-liquid extraction is different from the one you performed in Experiment 4, but it uses the same type of logic. Your task is to show how to separate apart Compound A and Compound B. . Complete the following flowchart of a liquid-liquid extraction. Handwritten work is encouraged. • Draw by hand (neatly) only the appropriate organic compound(s) in the boxes. . Specify the reagent(s)/chemicals (name is fine) and concentration as required in Boxes 4 and 5. • Box 7a requires the solvent (name is fine). • Box 7b requires one inorganic compound. • You can neatly complete this assignment by hand and…arrow_forwardb) Elucidate compound D w) mt at 170 nd shows c-1 stretch at 550cm;' The compound has the ff electronic transitions: 0%o* and no a* 1H NMR Spectrum (CDCl3, 400 MHz) 3.5 3.0 2.5 2.0 1.5 1.0 0.5 ppm 13C{H} NMR Spectrum (CDCl3, 100 MHz) Solvent 80 70 60 50 40 30 20 10 0 ppm ppm ¹H-13C me-HSQC Spectrum ppm (CDCl3, 400 MHz) 5 ¹H-¹H COSY Spectrum (CDCl3, 400 MHz) 0.5 10 3.5 3.0 2.5 2.0 1.5 1.0 10 15 20 20 25 30 30 -35 -1.0 1.5 -2.0 -2.5 3.0 -3.5 0.5 ppm 3.5 3.0 2.5 2.0 1.5 1.0 0.5 ppmarrow_forward
- Part I. a) Elucidate the structure of compound A using the following information. • mass spectrum: m+ = 102, m/2=57 312=29 • IR spectrum: 1002.5 % TRANSMITTANCE Ngg 50 40 30 20 90 80 70 60 MICRONS 5 8 9 10 12 13 14 15 16 19 1740 cm M 10 0 4000 3600 3200 2800 2400 2000 1800 1600 13 • CNMR 'H -NMR Peak 8 ppm (H) Integration multiplicity a 1.5 (3H) triplet b 1.3 1.5 (3H) triplet C 2.3 1 (2H) quartet d 4.1 1 (2H) quartet & ppm (c) 10 15 28 60 177 (C=0) b) Elucidate the structure of compound B using the following information 13C/DEPT NMR 150.9 MHz IIL 1400 WAVENUMBERS (CM-1) DEPT-90 DEPT-135 85 80 75 70 65 60 55 50 45 40 35 30 25 20 ppm 1200 1000 800 600 400arrow_forward• Part II. a) Elucidate The structure of compound c w/ molecular formula C10 11202 and the following data below: • IR spectra % TRANSMITTANCE 1002.5 90 80 70 60 50 40 30 20 10 0 4000 3600 3200 2800 2400 2000 1800 1600 • Information from 'HAMR MICRONS 8 9 10 11 14 15 16 19 25 1400 WAVENUMBERS (CM-1) 1200 1000 800 600 400 peak 8 ppm Integration multiplicity a 2.1 1.5 (3H) Singlet b 3.6 1 (2H) singlet с 3.8 1.5 (3H) Singlet d 6.8 1(2H) doublet 7.1 1(2H) doublet Information from 13C-nmR Normal carbon 29ppm Dept 135 Dept -90 + NO peak NO peak 50 ppm 55 ppm + NO peak 114 ppm t 126 ppm No peak NO peak 130 ppm t + 159 ppm No peak NO peak 207 ppm по реак NO peakarrow_forwardCould you redraw these and also explain how to solve them for me pleasarrow_forward
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